Indian Journal of Dermatology
CASE REPORT
Year
: 2007  |  Volume : 52  |  Issue : 1  |  Page : 53--55

Prolidase deficiency


Qazi Masood, Taseer Ahmed Bhatt, Iffat Hassan, Farah Sameen, Sabiya Majid 
 Department of Dermatology, STD, Leprosy and Biochemistry, Govt. Medical College, Srinagar, India

Correspondence Address:
Taseer Ahmed Bhatt
R/O:-Shabeer Manzil, Rajbagh Extension, Srinagar, Kashmir - 190 008 (J and K)
India

Prolidase deficiency is a rare inborn disorder of collagen metabolism characterized by chronic recurrent skin ulceration. A seven-year-old girl and her younger sibling with clinical features and laboratory criteria fulfilling the diagnosis of prolidase deficiency are presented in view of rarity of the condition.


How to cite this article:
Masood Q, Bhatt TA, Hassan I, Sameen F, Majid S. Prolidase deficiency.Indian J Dermatol 2007;52:53-55


How to cite this URL:
Masood Q, Bhatt TA, Hassan I, Sameen F, Majid S. Prolidase deficiency. Indian J Dermatol [serial online] 2007 [cited 2020 Dec 3 ];52:53-55
Available from: https://www.e-ijd.org/article.asp?issn=0019-5154;year=2007;volume=52;issue=1;spage=53;epage=55;aulast=Masood;type=0